Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

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31x24mm Implant 14mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-3114
In Commercial Distribution

  • 10889981038458 ()

  • 31x24mm, 14mm 12°
21-LT-3114

  • Bone-screw internal spinal fixation system, non-sterile
31x24mm Implant 12mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-3112
In Commercial Distribution

  • 10889981038441 ()

  • 31x24mm, 12mm 12°
21-LT-3112

  • Bone-screw internal spinal fixation system, non-sterile
31x24mm Implant 10mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-3110
In Commercial Distribution

  • 10889981038434 ()

  • 4.5 x 12mm
21-LT-3110

  • Bone-screw internal spinal fixation system, non-sterile
31x24mm Implant 8mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-3108
In Commercial Distribution

  • 10889981038427 ()

  • 4.5 x 10mm
21-LT-3108

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Implant 16mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-2716
In Commercial Distribution

  • 10889981038410 ()

  • 4.0 x 18mm
21-LT-2716

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Implant 14mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-2714
In Commercial Distribution

  • 10889981038403 ()

  • 4.0 x 16mm
21-LT-2714

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Implant 12mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-2712
In Commercial Distribution

  • 10889981038397 ()

  • 4.0 x 14mm
21-LT-2712

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Implant 10mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-2710
In Commercial Distribution

  • 10889981038380 ()

  • 4.0 x 12mm
21-LT-2710

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Implant 8mm 12 deg
SEASPINE ORTHOPEDICS CORPORATION
21-LT-2708
In Commercial Distribution

  • 10889981038373 ()

  • 4.0 x 10mm
21-LT-2708

  • Bone-screw internal spinal fixation system, non-sterile
27x21mm Trial 12mm 12 deg. The Vu a-POD intervertebral body fusion device is comprised of polymer (PEEK OPTIMA® LT) concave cages. The PEEK cages include tantalumpins (or radiopaque markers) for radiological evaluation. All pins are press fit into the PEEK material. The pins are placed in the implant on each end of the PEEK cages to allow easier radiological assessment of the position and orientation of the radiolucent PEEK cage.
SEASPINE ORTHOPEDICS CORPORATION
21-21-2712
In Commercial Distribution

  • 10889981038106 ()

  • 27x21mm 12mm 12°
21-21-2712

  • Bone-screw internal spinal fixation system, non-sterile
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